Carefusion recalls bipolar forceps with missing instructions for power supply and cleaning. Owners should check model numbers and contact Carefusion for details.
BD has determined that the Instructions For Use (IFU) provided by BD is missing certain content that is contained in the manufacturer's IFU. This missing content is related to the interface with the device power supply, as well as cleaning and maintenance instructions. Refer to the attached V. Mueller" Bipolar Forcep IFU.
Carefusion is recalling bipolar forceps that lack critical instructions for power supply and cleaning. This could lead to improper use if owners follow outdated or incomplete guidelines.
The forceps come with incomplete instructions for connecting to power supplies and cleaning. Without these details, users might connect improperly or clean incorrectly, potentially causing damage or injury.
Medical professionals using the forceps for procedures are most at risk. The recall affects specific model numbers sold with certain lot numbers.
Check for model number F-1303 and lot numbers on the packaging. The forceps have a specific length (7-1/2 inches) and 1.0mm tip.
Look for model number F-130:1303 on the packaging or product label.
Reach out to Carefusion for specific instructions on handling the recalled product.
The recall is due to missing instructions for power supply connection and cleaning, which could lead to improper use.
Check the model number and contact Carefusion for guidance on next steps.
The recall indicates incomplete instructions, but no specific injury risk is stated in the official notice.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0386-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0386-2023 from Carefusion. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
